drugset / Trial / NCT01058083

Safety Study of BMS-770767 in Subjects With Hypercholesterolemia

NCT01058083 ↗

Phase 2 Completed 81 enrolled Bristol-Myers Squibb
RandomizedParallel-groupTriple-blindTreatment

Summary

The purpose of this study is to assess the safety, tolerability and pharmacodynamic effects on LDL cholesterol (LDL-C)

Timeline

Start
2010-05
Primary completion
2011-03
Completion
2011-03

Drugs

EvaluationDrugModalityDoseRoute
Subject BMS-770767 Unknown 15 mg Oral
Subject BMS-770767 Unknown 50 mg Oral
Subject BMS-770767 Unknown 150 mg Oral

Indications